Nina Lanzarotti

546 total citations
3 papers, 166 citations indexed

About

Nina Lanzarotti is a scholar working on Immunology, Molecular Biology and Genetics. According to data from OpenAlex, Nina Lanzarotti has authored 3 papers receiving a total of 166 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Immunology, 2 papers in Molecular Biology and 1 paper in Genetics. Recurrent topics in Nina Lanzarotti's work include Immune Cell Function and Interaction (2 papers), Protein Tyrosine Phosphatases (1 paper) and Diabetes and associated disorders (1 paper). Nina Lanzarotti is often cited by papers focused on Immune Cell Function and Interaction (2 papers), Protein Tyrosine Phosphatases (1 paper) and Diabetes and associated disorders (1 paper). Nina Lanzarotti collaborates with scholars based in France, India and United Kingdom. Nina Lanzarotti's co-authors include Aude Magérus, Frédéric Rieux‐Laucat, Bénédicte Neven, Brigitte Bader‐Meunier, Capucine Pïcard, Hélène Cavé, Nadia Jeremiah, Alain Fischer, Valérie Cormier‐Daire and Marie‐Claude Stolzenberg and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Allergy and Clinical Immunology and Seminars in Arthritis and Rheumatism.

In The Last Decade

Nina Lanzarotti

3 papers receiving 165 citations

Peers

Nina Lanzarotti
Emily L. Blalock United States
Daniel M. Schreeder United States
Velia Gerl Germany
Judy Young United States
Jennifer Segar United States
Sophine Boysen Krintel Denmark
Aurélie De Groof Belgium
MA Brach Germany
Natalia S. Chaimowitz United States
Angela Rofelty United States
Emily L. Blalock United States
Nina Lanzarotti
Citations per year, relative to Nina Lanzarotti Nina Lanzarotti (= 1×) peers Emily L. Blalock

Countries citing papers authored by Nina Lanzarotti

Since Specialization
Citations

This map shows the geographic impact of Nina Lanzarotti's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Nina Lanzarotti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nina Lanzarotti more than expected).

Fields of papers citing papers by Nina Lanzarotti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nina Lanzarotti. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Nina Lanzarotti. The network helps show where Nina Lanzarotti may publish in the future.

Co-authorship network of co-authors of Nina Lanzarotti

This figure shows the co-authorship network connecting the top 25 collaborators of Nina Lanzarotti. A scholar is included among the top collaborators of Nina Lanzarotti based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Nina Lanzarotti. Nina Lanzarotti is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

3 of 3 papers shown
1.
Bader‐Meunier, Brigitte, Hélène Cavé, Nadia Jeremiah, et al.. (2013). Are RASopathies new monogenic predisposing conditions to the development of systemic lupus erythematosus? Case report and systematic review of the literature. Seminars in Arthritis and Rheumatism. 43(2). 217–219. 49 indexed citations
2.
Magérus, Aude, Marie‐Claude Stolzenberg, Nina Lanzarotti, et al.. (2012). Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation. Journal of Allergy and Clinical Immunology. 131(2). 486–490. 34 indexed citations
3.
Magérus, Aude, Bénédicte Neven, Marie‐Claude Stolzenberg, et al.. (2010). Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation. Journal of Clinical Investigation. 121(1). 106–112. 83 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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2026